A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5593551



Internal ID21542140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11885356..11885472hg38UCSC Ensembl
chr10:11927355..11927471hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068575
SamplesHG00731
Known GenesPROSER2-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5593551
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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